D-0743-2026 Class I Ongoing
FDA drug recall D-0743-2026 was initiated by Sunny Pharmtech Inc. on July 17, 2026 and is designated Class I. Reason for recall: Presence of Particulate Matter; identified as stainless steel The recall status is ongoing. Affected quantity: 4,077 vials.
Recall Details
- Product Type
- Drugs
- Report Date
- August 12, 2026
- Initiation Date
- July 17, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 4,077 vials
Product Description
Cyclophosphamide for Injection, USP, 1 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8112-1
Reason for Recall
Presence of Particulate Matter; identified as stainless steel
Distribution Pattern
USA Nationwide
Code Information
Lot # C23019V1, Exp 10/31/2026; C24015V1, Exp 4/30/2027